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61656-43-7

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61656-43-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61656-43-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,5 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61656-43:
(7*6)+(6*1)+(5*6)+(4*5)+(3*6)+(2*4)+(1*3)=127
127 % 10 = 7
So 61656-43-7 is a valid CAS Registry Number.

61656-43-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3-phenyl-1,2-oxazol-5-yl)propanoic acid

1.2 Other means of identification

Product number -
Other names 5-Isoxazolepropanoic acid,3-phenyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:61656-43-7 SDS

61656-43-7Relevant articles and documents

Synthesis and biological evaluation of fluoro-substituted spiro-isoxazolines as potential anti-viral and anti-cancer agents

Boone, Sarah,Das, Prasanta,Hamme, Ashton T.,Mitra, Dipanwita,Raucher, Drazen,Tandon, Ritesh,Turner, Lindsay

, p. 30223 - 30237 (2020/09/03)

Electrophilic fluorine-mediated dearomative spirocyclization has been developed to synthesize a range of fluoro-substituted spiro-isoxazoline ethers and lactones. The in vitro biological assays of synthesized compounds were probed for anti-viral activity

Oxonium ion-mediated synthesis of 4-substituted spiro-isoxazolines

McClendon, Eric,Omollo, Ann O.,Valente, Edward J.,Hamme II, Ashton T.

body text, p. 533 - 535 (2009/04/14)

The stereoselective synthesis of 4-bromo-spiro-isoxazolines was achieved in one step through the bromination of various isoxazoles that contain a pendant alcohol or carboxylic acid functional group. Isoxazole bromination leads to a bromonium ion intermedi

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